Canonical Allele Identifier: CA344834016
Community Standard Title: NM_206933.4(USH2A):c.14396C>A (p.Thr4799Asn)
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215648714G>T , CM000663.2:g.215648714G>T GRCh38
NC_000001.10:g.215822056G>T , CM000663.1:g.215822056G>T GRCh37
NC_000001.9:g.213888679G>T NCBI36
NG_009497.1:g.779683C>A
NG_009497.2:g.779735C>A

Transcript Alleles

HGVS Amino-acid Change
NM_206933.4:c.14396C>A MANE Select NP_996816.3:p.Thr4799Asn
ENST00000307340.8:c.14396C>A MANE Select ENSP00000305941.3:p.Thr4799Asn
NM_206933.2:c.14396C>A NP_996816.2:p.Thr4799Asn
NM_206933.3:c.14396C>A NP_996816.2:p.Thr4799Asn
ENST00000307340.7:c.14396C>A ENSP00000305941.3:p.Thr4799Asn
ENST00000674083.1:c.14396C>A ENSP00000501296.1:p.Thr4799Asn